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corneal
相关语句
  角膜
    Nursing Care for Corneal Intra Barrier Reconstruction
    角膜内屏障重建术的护理
短句来源
    Significance of corneal thickness changes measured by ultrasonic pachymeter after penetrating keratoplasty
    穿透性角膜移植术后超声测量角膜厚度的意义
短句来源
    Analysis of sFas and sFasL in some corneal disease
    房水sFas和sFasL在部分角膜疾病的分析
短句来源
    Influence of diagnostic ultrasound on corneal cell apoptosis in rats
    诊断超声对大鼠角膜细胞凋亡的影响
短句来源
    Nursing Care of Lamellar Keratoplasty with Amnion Transplantation for Mooren's Diseases Associated with Corneal Perforation
    1例板层角膜联合羊膜移植治疗Mooren’s病并角膜穿孔的护理
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  “corneal”译为未确定词的双语例句
    Nursing of Corneal Limbus Stem Cells Autografting Treatment for Pterygium Xin Chunyan Li Jian Wang Lijie
    角膜缘干细胞移植治疗翼状胬肉的护理
短句来源
    Nursing of Pterygium Cases Under the Combined Measure of Corneal Limbus stem Cell Transplantation and Mitomycin C
    角膜缘干细胞移植联合丝裂霉素C治疗翼状胬肉的护理
短句来源
    Nursing of 39 Recurrent Pterygium Cases with Amnion Transplantation Combined with Corneal Limbus Autotransplantation
    羊膜联合自体角膜缘移植治疗复发性翼状胬肉的护理39例
短句来源
    In model of rabbit Pseudomonas auruginosa corneal ulcer, the sensitivity of PCR was 93.8%, the specificity of PCR was 100%;
    动物模型 PCR敏感性为 93.8% ,特异性为 10 0 .0 % ;
短句来源
    Corneal cell reactions to laser ablation
    激光消融对角膜细胞的影响
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  corneal
The experimental results show that the integration of microsensors for microsurgery robot's end-effector can satisfy the design requirements, and the robotic end trephine can accurately fulfill the surgical task of corneal cutting.
      
Fast deposition of hydroxyapatite coating on titanium to modify cell affinity of corneal fibroblast in vitro
      
It is shown for the first time that HA coating can significantly enhance the adhesion and proliferation of rabbit corneal fibroblast in comparison with that of pure Ti.
      
We studied 56 biopsy samples of conjunctiva and 50 corneal discs excised from 28 patients with acquired keratoconus cornea.
      
Necrobiotic changes have been revealed in epithelium of the corneal discs going by the pathways of apoptosis-programmed cell death-and oncosis-initial edematic stage of necrobiosis.
      
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Authors used the low and high output nitrogen laser to irradiate the rabbit eyes. The chronic inflammation occurred on the limbus corneal proper, vi-treous body, retiaal and optic disc. Low output iriadiation group changes were found chiefly the lymphocytic infiltration along the corneal limbus and in the bulbae sub-conjunctival space together with some fibroblasts and newly formed blood vessels. The changes in the optic disc is more apparent on the high output irradiation group than the low output...

Authors used the low and high output nitrogen laser to irradiate the rabbit eyes. The chronic inflammation occurred on the limbus corneal proper, vi-treous body, retiaal and optic disc. Low output iriadiation group changes were found chiefly the lymphocytic infiltration along the corneal limbus and in the bulbae sub-conjunctival space together with some fibroblasts and newly formed blood vessels. The changes in the optic disc is more apparent on the high output irradiation group than the low output group. So that the nitrogen laser irradiation of rabbit eyes could induce chronic inflammation and risual cell damage of the eyes.

作者用高低功率N_2激光照射兔眼,发现角膜缘、角膜、玻璃体、视网膜和视乳头有慢性炎症。低功率组发现角膜缘球结膜下淋巴细胞浸润为主兼有成纤维细胞和新生血管。高功率组发现视网膜视乳头的改变比低功率明显。因此,N_2激光照射对兔眼可引起眼组织慢性炎症,并能损害视细胞。

ABSTRACT M ucopolysaccharidosis Ⅱ (MPS Ⅱ)and MPS Ⅰ are both characterized by gargoylist dwarfism. So, they are often confused. MPS Ⅱ only affects malepersons because of its X—linked recessive heredity. Five cases were found in three families, who were all the maternal grandsons. Through 10 years of investigation there are no such features as hunchback, corneal nebula and, hypointelligence in all the five cases. These are quitedifferent from those of MPS Ⅰ although they are quite similar in X—ray films....

ABSTRACT M ucopolysaccharidosis Ⅱ (MPS Ⅱ)and MPS Ⅰ are both characterized by gargoylist dwarfism. So, they are often confused. MPS Ⅱ only affects malepersons because of its X—linked recessive heredity. Five cases were found in three families, who were all the maternal grandsons. Through 10 years of investigation there are no such features as hunchback, corneal nebula and, hypointelligence in all the five cases. These are quitedifferent from those of MPS Ⅰ although they are quite similar in X—ray films. The important features of MPS Ⅱ are: butterfish—Like vertebrae; extrophia of the near part of humeri; calcanea become bucky in the middle part. metacarpus are thicker than that of ossa digtorum manus: carpal scaphoid and os naviculare appear tobe small and triangular malformation; soft tissues take onnodose image. All of the tyoical characters can be used to differentiate MPS Ⅱ from MPS Ⅰ.

粘多糖病(MPs)Ⅱ型(Hunter Syndrome)与I型(Hurler Syndrome)在临床上都表现为承溜侏儒,常易混淆,但粘多糖病Ⅱ型系X连锁隐性遗传,只见于男性。本组5例同属一个母系的三个家庭,经10年观察,无角膜混浊及驼背现象,智力低下不明显。X线征虽与Ⅰ型有共同之处,但毕竟有区别,其中鲳鱼状椎骨、肱骨近端外翻、指骨比掌骨粗、跟骨腰部增粗,腕舟、跗舟骨细小呈三角状变形及软组织结节影等都是Ⅱ型的特征,可作为两者鉴别诊断时的参考。

Twenty-four patients with mucopolysaccharidosis(MPS) were studied. our series includes 15 cases of MPS I-Hurler's syndrome and 9 cases of MPS Ⅵ ( Morqnio's syndrome ). The patients, both of type Ⅰ and type Ⅳ, showed increased urinary excretion of acid mucopolysccharide and were confirmed by biochemical and peripheral blood piture tests. There were typical features in all of them both clinically and radiologically. In MPSI-H, the clinic features are: facial coarseness ugliness ( "gargoylism or tumorlike"), corneal...

Twenty-four patients with mucopolysaccharidosis(MPS) were studied. our series includes 15 cases of MPS I-Hurler's syndrome and 9 cases of MPS Ⅵ ( Morqnio's syndrome ). The patients, both of type Ⅰ and type Ⅳ, showed increased urinary excretion of acid mucopolysccharide and were confirmed by biochemical and peripheral blood piture tests. There were typical features in all of them both clinically and radiologically. In MPSI-H, the clinic features are: facial coarseness ugliness ( "gargoylism or tumorlike"), corneal cloudiness, mental redardation, and marked hepatosplenomegaly. The X-ray signs are: an enlarged skull, giving a scaphocephalic shape, enlarged J-shaped sella turcica, thoraco-lumbar vertebrae becoming "hooked-like" in there anteroinferior borders and impalement of diaphyseal modelling. In MPS Ⅵ ( Morquio's syndrome ) the main clinic features are: basically normal intelligence and bowleg (genu varum) deformities associated with joints laxity. The X-ray findings are: normal skull and sella turcica, vertebrae becoming flat ( platyspondylia ) with a central tongue-like protrusion at its anterior margin. The radiological diagnosis and differdntial diagnosis are also discussed.

本文报告24例粘多糖病,其中MPSI-Hurler 15例,MPSⅣ-Morguio9例,均经尿液生化或周围血象检查证实,并有典型的临床和X线表现.MPSI-Hurler的症状有:面丑(呈瘤样),角膜混浊,智力低下及肝、脾肿大等.X线表现有:头大、舟状畸形,蝶鞍呈J-形,胸-腰段椎体前下缘变尖呈钩形,长骨骨干常有塑形障碍.MPSⅣ-Morguio的主要临床表现是:智力基本正常,有明显的膝内翻和关节松弛.X线征象有:椎体变扁(扁平椎),其前缘正中呈舌样突出.并讨论了其X线诊断和鉴别诊断.

 
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